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1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione

In the title compound, C(41)H(31)N(3)O(3), the pyrazole and pyrrolidine rings adopt twisted conformations. The mean plane of the pyrazole ring forms dihedral angles of 9.11 (12) and 39.65 (11)° with the phenyl rings. The O atoms deviate from the mean planes of the chromene and ace­naphthyl­ene ring...

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Autores principales: Jagadeesan, G., Kathirvelan, D., Haribabu, J., Reddy, B. S. R., Sethusankar, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648244/
https://www.ncbi.nlm.nih.gov/pubmed/23723864
http://dx.doi.org/10.1107/S1600536813009562
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author Jagadeesan, G.
Kathirvelan, D.
Haribabu, J.
Reddy, B. S. R.
Sethusankar, K.
author_facet Jagadeesan, G.
Kathirvelan, D.
Haribabu, J.
Reddy, B. S. R.
Sethusankar, K.
author_sort Jagadeesan, G.
collection PubMed
description In the title compound, C(41)H(31)N(3)O(3), the pyrazole and pyrrolidine rings adopt twisted conformations. The mean plane of the pyrazole ring forms dihedral angles of 9.11 (12) and 39.65 (11)° with the phenyl rings. The O atoms deviate from the mean planes of the chromene and ace­naphthyl­ene ring systems by 0.194 (15) and 0.079 (15) Å, respectively. In the crystal, molecules are linked via pairs of C—H⋯O inter­actions,forming inversion dimers with an R (2) (2)(12) ring motif.
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spelling pubmed-36482442013-05-30 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione Jagadeesan, G. Kathirvelan, D. Haribabu, J. Reddy, B. S. R. Sethusankar, K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(41)H(31)N(3)O(3), the pyrazole and pyrrolidine rings adopt twisted conformations. The mean plane of the pyrazole ring forms dihedral angles of 9.11 (12) and 39.65 (11)° with the phenyl rings. The O atoms deviate from the mean planes of the chromene and ace­naphthyl­ene ring systems by 0.194 (15) and 0.079 (15) Å, respectively. In the crystal, molecules are linked via pairs of C—H⋯O inter­actions,forming inversion dimers with an R (2) (2)(12) ring motif. International Union of Crystallography 2013-04-13 /pmc/articles/PMC3648244/ /pubmed/23723864 http://dx.doi.org/10.1107/S1600536813009562 Text en © Jagadeesan et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Jagadeesan, G.
Kathirvelan, D.
Haribabu, J.
Reddy, B. S. R.
Sethusankar, K.
1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title_full 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title_fullStr 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title_full_unstemmed 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title_short 1′-(1,3-Diphenyl-1H-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′H-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1H)-dione
title_sort 1′-(1,3-diphenyl-1h-pyrazol-4-yl)-2′,3′,5′,6′,7′,7a’-hexa­hydro-1′h-di­spiro­[ace­naphthyl­ene-1,3′-pyrrolizine-2′,3′′-chromane]-2,4′′(1h)-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648244/
https://www.ncbi.nlm.nih.gov/pubmed/23723864
http://dx.doi.org/10.1107/S1600536813009562
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